Literature DB >> 8780771

Growth rate regulation of 4.5 S RNA and M1 RNA the catalytic subunit of Escherichia coli RNase P.

H Dong1, L A Kirsebom, L Nilsson.   

Abstract

We have studied the expression of 4.5 S RNA and M1 RNA, the catalytic subunit of Escherchia coli RNase P, under various growth conditions. Both RNA species increase in abundance as a function of growth rate. There are roughly 450 molecules of 4.5 S RNA and 80 molecules of M1 RNA per cell at 0.4 doubling per hour, and this is increased to 5300 and 1060 molecules per cell, respectively, at 2.7 doublings per hour. Deletion of both relA and spoT, the two genes that are responsible for synthesis of ppGpp, does not affect the rate of synthesis of either RNA species. However, deletion of fis renders the expression of 4.5 S RNA independent of growth rate, but has little effect on the expression of M1 RNA. These data suggest that the expression of both 4.5 S RNA and M1 RNA genes are growth-rate regulated, but not through the same mechanism. The growth-rate dependent accumulation of 4.5 S RNA depends on FIS-mediated trans-activation, whereas that of M1 RNA is not governed by ppGpp or by FIS.

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Year:  1996        PMID: 8780771     DOI: 10.1006/jmbi.1996.0461

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  20 in total

1.  Activation of Escherichia coli leuV transcription by FIS.

Authors:  W Ross; J Salomon; W M Holmes; R L Gourse
Journal:  J Bacteriol       Date:  1999-06       Impact factor: 3.490

2.  Positive growth rate-dependent regulation of the pdxA, ksgA, and pdxB genes of Escherichia coli K-12.

Authors:  Andrew J Pease; Benjamin R Roa; Wen Luo; Malcolm E Winkler
Journal:  J Bacteriol       Date:  2002-03       Impact factor: 3.490

Review 3.  Linkage map of Escherichia coli K-12, edition 10: the traditional map.

Authors:  M K Berlyn
Journal:  Microbiol Mol Biol Rev       Date:  1998-09       Impact factor: 11.056

4.  Essential is not irreplaceable: fitness dynamics of experimental E. coli RNase P RNA heterologous replacement.

Authors:  Jasmine L Loveland; Jocelyn Rice; Paula C G Turrini; Michelle Lizotte-Waniewski; Robert L Dorit
Journal:  J Mol Evol       Date:  2014-09-30       Impact factor: 2.395

5.  Protein-only RNase P function in Escherichia coli: viability, processing defects and differences between PRORP isoenzymes.

Authors:  Markus Gößringer; Marcus Lechner; Nadia Brillante; Christoph Weber; Walter Rossmanith; Roland K Hartmann
Journal:  Nucleic Acids Res       Date:  2017-07-07       Impact factor: 16.971

6.  Lon Protease Removes Excess Signal Recognition Particle Protein in Escherichia coli.

Authors:  Beate Sauerbrei; Jan Arends; Danja Schünemann; Franz Narberhaus
Journal:  J Bacteriol       Date:  2020-06-25       Impact factor: 3.490

7.  Analysis of RNase P protein (rnpA) expression in Bacillus subtilis utilizing strains with suppressible rnpA expression.

Authors:  Markus Gössringer; Rosel Kretschmer-Kazemi Far; Roland K Hartmann
Journal:  J Bacteriol       Date:  2006-10       Impact factor: 3.490

8.  Regulation of rRNA transcription is remarkably robust: FIS compensates for altered nucleoside triphosphate sensing by mutant RNA polymerases at Escherichia coli rrn P1 promoters.

Authors:  M S Bartlett; T Gaal; W Ross; R L Gourse
Journal:  J Bacteriol       Date:  2000-04       Impact factor: 3.490

9.  Downregulation of the Escherichia coli guaB promoter by FIS.

Authors:  Seyyed I Husnain; Mark S Thomas
Journal:  Microbiology (Reading)       Date:  2008-06       Impact factor: 2.777

10.  Downregulation of the Escherichia coli guaB promoter by upstream-bound cyclic AMP receptor protein.

Authors:  Seyyed I Husnain; Stephen J W Busby; Mark S Thomas
Journal:  J Bacteriol       Date:  2009-07-24       Impact factor: 3.490

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